Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs2129098891
- Species
- Homo sapiens
- Symbol
- rs2129098891
- Category
- Variant
- Variant type
- SNP
- Overlaps
- KMT2C
- Location
- 7:152154463
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_000007.14:g.152154463C>T
- HGVS.c name
- ENSEMBL:ENST00000262189.11:c.11961-18G>A
- ENSEMBL:ENST00000355193.1:c.12180-18G>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr7:152134922...152436644 (301.72 kb)
- Assembly version
- Not Available
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